loading...| Preferred Name | Spinocerebellar Degenerations | |
| Synonyms |
Ataxias, Hereditary Degeneration, Corticostriatal-Spinal Corticostriatal Spinal Degeneration Degenerations, Familial Spinocerebellar Degeneration, Inherited Spinocerebellar Corticostriatal-Spinal Degenerations Spino Cerebellar Degenerations Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism Cerebellar Degeneration, Primary Syndrome, Marinesco-Garland Spinocerebellar Disease Spinocerebellar Degenerations, Familial Spinocerebellar Degeneration, Familial Cerebellar Degenerations, Primary Marie's Cerebellar Ataxia Degeneration, Spino-Cerebellar Corticostriatal-Spinal Degeneration Hereditary Oligophrenic Cerebello Lental Degeneration Syndrome, Garland-Moorhouse Marinesco-Sjogren Syndrome Degenerations, Hereditary Spinocerebellar Degeneration, Spino Cerebellar Inherited Spinocerebellar Degeneration Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren Marinesco-Sjogren-Garland Syndrome Marie Cerebellar Ataxia Spinocerebellar Degenerations, Inherited Syndrome, Marinesco-Sjögren Spinocerebellar Diseases Degeneration, Primary Cerebellar Hereditary Oligophrenic Cerebello-Lental Degeneration Syndrome-Myopathy, Marinesco-Sjogren Marinesco-Sjogren Syndrome-Myopathy Cerebellar Ataxia, Marie's Familial Spinocerebellar Degenerations Marinesco Sjogren Garland Syndrome Degenerations, Corticostriatal-Spinal Marinesco Sjögren Syndrome Hereditary Spinocerebellar Degenerations Degenerations, Spino Cerebellar Degenerations, Spinocerebellar Spinocerebellar Degeneration, Hereditary Marinesco Sjogren Syndrome Myopathy Marinesco-Sjögren Syndrome Syndrome, Marinesco-Sjogren-Garland Garland Moorhouse Syndrome Primary Cerebellar Degenerations Spinocerebellar Degeneration Marinesco Sjogren Syndrome Inherited Spinocerebellar Degenerations Spino-Cerebellar Degeneration Hereditary Ataxias Hereditary Ataxia Late Onset Cerebellar Ataxia Spino-Cerebellar Degenerations Degeneration, Spinocerebellar Garland-Moorhouse Syndrome Cerebellar Ataxia, Late Onset Early Onset Cerebellar Ataxia Degeneration, Familial Spinocerebellar Degenerations, Inherited Spinocerebellar Spinocerebellar Degenerations, Hereditary Degeneration, Hereditary Spinocerebellar Degenerations, Primary Cerebellar Hereditary Spinocerebellar Degeneration Marinesco Garland Syndrome Ataxia, Hereditary Spinocerebellar Degeneration, Inherited Cerebellar Ataxia, Marie Syndrome, Marinesco-Sjogren Cerebellar Ataxia, Early Onset Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic Spino Cerebellar Degeneration Primary Cerebellar Degeneration Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism Marinesco-Garland Syndrome Familial Spinocerebellar Degeneration |
|
| Definitions |
A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. |
|
| ID |
http://purl.bioontology.org/ontology/MESH/D013132 |
|
| altLabel |
Ataxias, Hereditary Degeneration, Corticostriatal-Spinal Corticostriatal Spinal Degeneration Degenerations, Familial Spinocerebellar Degeneration, Inherited Spinocerebellar Corticostriatal-Spinal Degenerations Spino Cerebellar Degenerations Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism Cerebellar Degeneration, Primary Syndrome, Marinesco-Garland Spinocerebellar Disease Spinocerebellar Degenerations, Familial Spinocerebellar Degeneration, Familial Cerebellar Degenerations, Primary Marie's Cerebellar Ataxia Degeneration, Spino-Cerebellar Corticostriatal-Spinal Degeneration Hereditary Oligophrenic Cerebello Lental Degeneration Syndrome, Garland-Moorhouse Marinesco-Sjogren Syndrome Degenerations, Hereditary Spinocerebellar Degeneration, Spino Cerebellar Inherited Spinocerebellar Degeneration Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren Marinesco-Sjogren-Garland Syndrome Marie Cerebellar Ataxia Spinocerebellar Degenerations, Inherited Syndrome, Marinesco-Sjögren Spinocerebellar Diseases Degeneration, Primary Cerebellar Hereditary Oligophrenic Cerebello-Lental Degeneration Syndrome-Myopathy, Marinesco-Sjogren Marinesco-Sjogren Syndrome-Myopathy Cerebellar Ataxia, Marie's Familial Spinocerebellar Degenerations Marinesco Sjogren Garland Syndrome Degenerations, Corticostriatal-Spinal Marinesco Sjögren Syndrome Hereditary Spinocerebellar Degenerations Degenerations, Spino Cerebellar Degenerations, Spinocerebellar Spinocerebellar Degeneration, Hereditary Marinesco Sjogren Syndrome Myopathy Marinesco-Sjögren Syndrome Syndrome, Marinesco-Sjogren-Garland Garland Moorhouse Syndrome Primary Cerebellar Degenerations Spinocerebellar Degeneration Marinesco Sjogren Syndrome Inherited Spinocerebellar Degenerations Spino-Cerebellar Degeneration Hereditary Ataxias Hereditary Ataxia Late Onset Cerebellar Ataxia Spino-Cerebellar Degenerations Degeneration, Spinocerebellar Garland-Moorhouse Syndrome Cerebellar Ataxia, Late Onset Early Onset Cerebellar Ataxia Degeneration, Familial Spinocerebellar Degenerations, Inherited Spinocerebellar Spinocerebellar Degenerations, Hereditary Degeneration, Hereditary Spinocerebellar Degenerations, Primary Cerebellar Hereditary Spinocerebellar Degeneration Marinesco Garland Syndrome Ataxia, Hereditary Spinocerebellar Degeneration, Inherited Cerebellar Ataxia, Marie Syndrome, Marinesco-Sjogren Cerebellar Ataxia, Early Onset Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic Spino Cerebellar Degeneration Primary Cerebellar Degeneration Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism Marinesco-Garland Syndrome Familial Spinocerebellar Degeneration |
|
| AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
|
| cui |
C0004138 C0393524 C0037952 C0024814 C0393519 C0270749 C0033132 C0270755 |
|
| DC |
1 |
|
| definition |
A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. |
|
| DX |
19870101 |
|
| HN |
2000(1987) |
|
| Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
| Machine permutation |
2000; see SPINOCEREBELLAR DEGENERATION 1989-1999, see SPINOCEREBELLAR DEGENERATIONS 1987-1988 |
|
| Mapped from |
http://purl.bioontology.org/ontology/MESH/C536342 http://purl.bioontology.org/ontology/MESH/C564264 http://purl.bioontology.org/ontology/MESH/C536989 http://purl.bioontology.org/ontology/MESH/C535472 http://purl.bioontology.org/ontology/MESH/C565865 http://purl.bioontology.org/ontology/MESH/C537204 http://purl.bioontology.org/ontology/MESH/C537206 http://purl.bioontology.org/ontology/MESH/C537200 http://purl.bioontology.org/ontology/MESH/C537201 http://purl.bioontology.org/ontology/MESH/C537198 http://purl.bioontology.org/ontology/MESH/C537197 http://purl.bioontology.org/ontology/MESH/C537309 http://purl.bioontology.org/ontology/MESH/C537307 http://purl.bioontology.org/ontology/MESH/C542540 http://purl.bioontology.org/ontology/MESH/C531684 http://purl.bioontology.org/ontology/MESH/C535523 http://purl.bioontology.org/ontology/MESH/C537312 http://purl.bioontology.org/ontology/MESH/C537311 http://purl.bioontology.org/ontology/MESH/C537310 http://purl.bioontology.org/ontology/MESH/C537313 |
|
| MDA |
19860331 |
|
| MMR |
20130708 |
|
| MN |
C10.574.500.825 C16.320.400.780 C10.228.854.787 C10.228.140.252.700 |
|
| notation |
D013132 |
|
| prefLabel |
Spinocerebellar Degenerations |
|
| TERMUI |
T370689 T370695 T038627 T370691 T746359 T364820 T370698 T370700 T370692 T370693 T370697 T746361 T370696 T746360 T841962 T038626 T038624 T370699 T746362 T370690 T038623 T038625 T841960 T370694 T841961 |
|
| TH |
OMIM (2013) NLM (2000) NLM (2012) NLM (1987) UNK (19XX) GHR (2014) ORD (2010) |
|
| tui |
T047 |
|
| subClassOf |
http://purl.bioontology.org/ontology/MESH/D002526 |